Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
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Acute Bilateral Inferior Cerebellar Infarction in a Patient With Neurosyphillis
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000
Retinocochleocerebral Vasculopathy
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Susac Syndrome
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Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
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Mitochondrial DNA and Disease
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Neurologic Manifestations of Giant Cell Arteritis
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Niemann-Pick Type C Disease
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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Niemann-Pick Disease Type C
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Wernekinck Commissure Syndrome
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More Than a Little Unsteady
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Adult-Onset Niemann-Pick Disease Type C Masquerading As Spinocerebellar Ataxias
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Autoimmune Nodopathies, An Emerging Dignostic Category
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A Triad of Tremor, Ataxia, and Cognitive Impairment
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Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
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A 57-Year-Old Woman with Progressive Ataxia and Falls
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
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Neurosyphilis
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
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Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Cerebellar Ataxia and Hearing Impairment
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A Woman in Her 60s with Chronic Meningitis from Aspergillus
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Clinical Manifestations of the anti-IgLON5 Disease
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A 54-year-old woman with Dementia, Myoclonus, and Ataxia
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A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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An 82-year-old man with Worsening Gait
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Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
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Cognitive Impairment Profile in adult Patients with Neimnn Pick Type C Disease
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Reversible Cognitive Decline Diagnosed on Ear Examination
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Atypical Presentations of Intracranial Hypotension: Comparison with Classic Spontaneous Intracranial Hypotension
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Extraintestinal Manifestations of Coeliac Disease
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Progressive Cerebellar Ataxia and New-Onset Diabetes
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Progressive Neuropsychiatric Symptoms and Motor Impairment
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